Synthesis of Backbone Thermo and pH Dual-Responsve Hyperbranched Poly(amine-ether)s Through Proton-Transfer Polymerization

被引:26
作者
Pang, Yan [1 ]
Zhu, Qi [1 ]
Zhou, Dongliang [2 ]
Liu, Jinyao [1 ]
Chen, Yan [1 ]
Su, Yue [3 ]
Yan, Deyue [1 ]
Zhu, Xinyuan [1 ,3 ]
Zhu, Bangshang [3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[2] Jiangsu Res Inst Bldg Sci Co Ltd, Nanjing 211103, Peoples R China
[3] Shanghai Jiao Tong Univ, Instrumental Anal Ctr, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
biocompatibility; hyperbranched; proton-transfer polymerization; stimuli-responsive polymers; stimuli-sensitive polymers; POLY(AMIDOAMINE) DENDRIMERS; POLYMERS; COPOLYMERS; POLYAMIDOAMINE; PROTEIN; VINYL; GELS;
D O I
10.1002/pola.24509
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Stimuli-responsive hyperbranched polymers have attracted great attention in recent years because of their wide applications in biomedicine. Through proton-transfer polymerization of triethanolamine and 1,2,7,8-diepoxyoctane with the help of potassium hydride, a series of novel backbone therm and pH dual-responsive hyperbranched poly(amine-ether)s were prepared successfully in one-pot. The degrees of branching of the resulting polymers were at 0.40-0.49. Turbidity measurements revealed that hyperbranched poly(amine-ether)s exhibited therm and pH dual-responsive properties in water. importantly, these responsivities could be readily adjusted by changing the polymer composition as well as the polymer con-centration in aqueous solution. Moreover, in vitro evaluation demonstrated that hyperbranched poly(amine-ether)s showed low cytotoxicity and efficient cell internalization against NIH 3T3 cell lines. These results suggest that these backbone therm and pH dual-responsive hyperbranched poly(amineether)s are promising materials for biomedicine. (C) 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 49: 966-975, 2011
引用
收藏
页码:966 / 975
页数:10
相关论文
共 57 条
[1]  
Bosman A. W., 1997, CHEM REV, V97, P1681
[2]   Temperature-responsive gels and thermogelling polymer matrices for protein and peptide delivery [J].
Bromberg, LE ;
Ron, ES .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 31 (03) :197-221
[3]   Dendritic Polyglycerols for Biomedical Applications [J].
Calderon, Marcelo ;
Quadir, Mohiuddin Abdul ;
Sharma, Sunil Kumar ;
Haag, Rainer .
ADVANCED MATERIALS, 2010, 22 (02) :190-218
[4]   New methodologies in the construction of dendritic materials [J].
Carlmark, Anna ;
Hawker, Craig J. ;
Hult, Anders ;
Malkoch, Michael .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (02) :352-362
[5]   Highly branched stimuli responsive poly [(N-isopropyl acrylamide)-co-(1,2-propandiol-3-methacrylate)]s with protein binding functionality [J].
Carter, S ;
Rimmer, S ;
Sturdy, A ;
Webb, M .
MACROMOLECULAR BIOSCIENCE, 2005, 5 (05) :373-378
[6]   Highly branched poly(N-isopropylacrylamide)s with imidazole end groups prepared by radical polymerization in the presence of a styryl monomer containing a dithioester group [J].
Carter, S ;
Hunt, B ;
Rimmer, S .
MACROMOLECULES, 2005, 38 (11) :4595-4603
[7]   Proton-transfer polymerization:: A new approach to hyperbranched polymers [J].
Chang, HT ;
Fréchet, JMJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (10) :2313-2314
[8]   Smart polymeric gels: Redefining the limits of biomedical devices [J].
Chaterji, Somali ;
Kwon, Il Keun ;
Park, Kinam .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (8-9) :1083-1122
[9]   Thermo-responsive highly branched polyethers by proton-transfer polymerization of 1,2,7,8-diepoxyoctane and multiols [J].
Chen, Hao ;
Jia, Zhifeng ;
Yan, Deyue ;
Zhu, Xinyuan .
MACROMOLECULAR CHEMISTRY AND PHYSICS, 2007, 208 (15) :1637-1645
[10]   Controlling polymer architecture through host-guest interactions [J].
Chen, L ;
Zhu, XY ;
Yan, DY ;
Chen, Y ;
Chen, Q ;
Yao, YF .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (01) :87-90